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Scientific Writer & Quality Medical Reviewer Job at Indegene

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Indegene is a technology-led healthcare solutions provider dedicated to making healthcare organizations future-ready. With a strong focus on innovation, collaboration, and customer-centric solutions, Indegene offers global growth opportunities for professionals passionate about the intersection of healthcare and technology.

Why Join Indegene?

  • Work at the cutting edge of healthcare and technology.
  • Fast-track career growth in a dynamic, purpose-driven environment.
  • Learn from industry experts and work on diverse projects across regulatory, medical affairs, and commercial solutions.
  • Be part of a culture that values entrepreneurship, innovation, and empathy.

Job Description: Scientific Writer & Quality Medical Reviewer

Key Responsibilities:

✔ Medical & Scientific Content Review:

  • Ensure compliance with MCA guidelines, data accuracy, and proper referencing.
  • Validate scientific information against cited references.
  • Check for consistency with approved product labeling and avoid off-label communication.

✔ Quality Assurance & Fact-Checking:

  • Verify reference quality, citation style, and contextual accuracy.
  • Ensure essential details (brand/generic names, AE reporting, API mentions) are included.

✔ Stakeholder Collaboration:

  • Work closely with Medical Affairs, clients, and cross-functional teams.
  • Defend content based on scientific evidence and provide clarifications.

✔ Therapeutic Expertise:

  • Write and review content across multiple therapy areas.
  • Stay updated on product knowledge and industry guidelines.

Requirements:

  • Advanced degree in Biosciences, Pharmacy, or Medicine (MD/PharmD/MSc/PhD).
  • 2-4 years of experience in medical writing, medical review, or medical affairs (pharma/healthcare).
  • Strong scientific acumen with the ability to grasp complex therapeutic topics.
  • Excellent written & verbal communication skills.
  • Familiarity with regulatory guidelines (MCA, FDA, etc.) is a plus.

Application Link

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